돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35884생성일: 2026년 10월 25일

1-(4-Phenylsulfonylphenyl)-3-hydroxy-3-methyl-4,4,4-trifluorobut-1-yne → 4,4,4-Trifluoro-3-hydroxy-3-methyl-1-(4-phenylsulfonylphenyl)-trans-but-1-ene

https://huagongshe.com/reaction/35884

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-Phenylsulfonylphenyl)-3-hydroxy-3-methyl-4,4,4-trifluorobut-1-yneHCID 19939303—
반응물Sodium bis(2-methoxyethoxy)aluminiumhydrideHCID 21584525—
용매Diethyl EtherHCID 3283—
생성물4,4,4-Trifluoro-3-hydroxy-3-methyl-1-(4-phenylsulfonylphenyl)-trans-but-1-eneHCID 986350779%

반응 단계

To a solution of sodium bis(2-methoxyethoxy)aluminum hydride (1.5 mL, 3.4M in toluene) in freshly distilled diethyl ether (6 mL) was added a solution of 1-(4-phenylsulfonylphenyl)-3-hydroxy-3-methyl-4,4,4-trifluorobut-1-yne in diethyl ether (6 mL) dropwise. The rate of addition was controlled so that the reaction temperature did not exceed 8° C. The mixture was stirred for 15 minutes and was quenched at 0° C. with 3N sulfuric acid (15 mL). Water (10 mL) was added and the product was extracted into diethyl ether. The combined organic extracts were washed (brine) and dried. The solvent was evaporated and the material was purified by chromatography, with chloroform:diethyl ether (25:1) as the eluent, to give the title compound (848 mg, 79%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05411973
출처 데이터셋uspto-grants-1995_05
ORD IDord-3e72d68742ee4716988a5c53520c7d6c
출처 메모uspto-grants-1995_05